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首页> 外文期刊>Receptors and channels >Alpha-adrenoceptor stimulation induces hypertrophy and increases L-type calcium current density in neonatal rat ventricular cardiomyocytes in culture.
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Alpha-adrenoceptor stimulation induces hypertrophy and increases L-type calcium current density in neonatal rat ventricular cardiomyocytes in culture.

机译:α-肾上腺素受体刺激诱导培养的新生大鼠心室心肌细胞肥大并增加L型钙电流密度。

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摘要

Effects of chronic alpha-adrenoceptor stimulation on hypertrophy and L-type calcium current (I(Ca-L) ) were investigated in neonatal rat ventricular cardiomyocytes in culture using whole-cell patch-clamp technique and measurement of protein- and RNA-to-DNA ratios. Chronic exposure to norepinephrine (2 microM) plus propranolol (2 microM) of cardiomyocytes during 1 and 3 days in culture increased cell membrane capacitance, protein- and RNA-to DNA ratios and was accompanied by an increase in I(Ca-L) density. These effects were not observed in the presence of prazosin (2 microM) suggesting that they could be due to alpha(1) -adrenoceptor stimulation. They were also prevented by cycloheximide (5 microM) and actinomycin D (1 microM). These effects were not observed in 1 and 3 day-cultured cells pre-treated for only 1 hour with norepinephrine. They were potentiated when calcium concentration was increased in the culture medium and, in contrast they were abolished in the presence of the L-type calcium current inhibitor, nifedipine (2 microM). The present study demonstrates that hypertrophy induced by long-term stimulation of alpha(1) -adrenoceptors is accompanied by an increase in the expression of functional calcium channels in neonatal rat cardiomyocytes. These results reveal the existence of a novel alpha(1) -mediated positive regulation of L-type calcium current different from that due to acute stimulation of alpha(1) -adrenoceptors in neonatal ventricular cardiomyocytes.
机译:使用全细胞膜片钳技术并测量蛋白质和RNA的量,研究了慢性α-肾上腺素受体刺激对新生大鼠心室心肌细胞肥大和L型钙电流(I(Ca-L))的影响。 DNA比率。在培养的第1天和第3天长期暴露于去甲肾上腺素(2 microM)加普萘洛尔(2 microM)的心肌细胞中,细胞膜电容,蛋白质和RNA与DNA的比率增加,并伴随I(Ca-L)密度的增加。在存在prazosin(2 microM)时未观察到这些影响,表明它们可能是由于alpha(1)-肾上腺素受体刺激所致。它们也被环己酰亚胺(5 microM)和放线菌素D(1 microM)预防。在用去甲肾上腺素仅预处理1小时的1和3天培养的细胞中未观察到这些作用。当培养基中的钙浓度增加时,它们被增强。相反,在存在L型钙电流抑制剂硝苯地平(2 microM)的情况下,它们被消除了。本研究表明,长期刺激α(1)-肾上腺素能受体诱发的肥大伴有新生大鼠心肌细胞中功能性钙通道表达的增加。这些结果揭示了新型α(1)介导的L型钙电流的正调控的存在,不同于由于急性心室心肌细胞对α(1)肾上腺素能受体的急性刺激所致。

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